Canonical Allele Identifier: CA1905809461
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43106324G= , CM000672.2:g.43106324G= GRCh38
NC_000010.10:g.43601772G= , CM000672.1:g.43601772G= GRCh37
NC_000010.9:g.42921778G= NCBI36
NG_007489.1:g.34256G= , LRG_518:g.34256G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.867+1131G= ENSP00000480088.2:n.867+1131G=
ENST00000683007.1:n.442-52G=
ENST00000340058.6:c.868-52G= ENSP00000344798.4:n.868-52G=
ENST00000355710.8:c.868-52G= MANE Select ENSP00000347942.3:n.868-52G=
ENST00000671844.1:c.625+3695G= ENSP00000500541.1:n.625+3695G=
ENST00000672389.1:c.74-4883G= ENSP00000500252.1:n.74-4883G=
ENST00000340058.5:c.868-52G= ENSP00000344798.4:n.868-52G=
ENST00000355710.7:c.868-52G= ENSP00000347942.3:n.868-52G=
ENST00000479913.1:n.463-52G=
ENST00000498820.5:c.74-5775G= ENSP00000419080.1:n.74-5775G=
ENST00000615310.4:c.868-52G= ENSP00000480088.1:n.868-52G=
NM_020630.4:c.868-52G= , LRG_518t2:c.868-52G= NP_065681.1:n.868-52G=
NM_020975.4:c.868-52G= , LRG_518t1:c.868-52G= NP_066124.1:n.868-52G=
XM_011540027.1:c.868-52G= XP_011538329.1:n.868-52G=
NM_001355216.1:c.106-52G= NP_001342145.1:n.106-52G=
NM_020630.5:c.868-52G= NP_065681.1:n.868-52G=
NM_020975.5:c.868-52G= NP_066124.1:n.868-52G=
NM_020975.6:c.868-52G= MANE Select NP_066124.1:n.868-52G=
NM_020630.6:c.868-52G= NP_065681.1:n.868-52G=